Optimized glycemic control of type 2 diabetes with reinforcement learning: a proof-of-concept trial.
Guangyu WangXiaohong LiuZhen YingGuoxing YangZhiwei ChenZhiwen LiuMin ZhangHongmei YanYuxing LuYuanxu GaoKanmin XueXiaoying LiYing ChenPublished in: Nature medicine (2023)
The personalized titration and optimization of insulin regimens for treatment of type 2 diabetes (T2D) are resource-demanding healthcare tasks. Here we propose a model-based reinforcement learning (RL) framework (called RL-DITR), which learns the optimal insulin regimen by analyzing glycemic state rewards through patient model interactions. When evaluated during the development phase for managing hospitalized patients with T2D, RL-DITR achieved superior insulin titration optimization (mean absolute error (MAE) of 1.10 ± 0.03 U) compared to other deep learning models and standard clinical methods. We performed a stepwise clinical validation of the artificial intelligence system from simulation to deployment, demonstrating better performance in glycemic control in inpatients compared to junior and intermediate-level physicians through quantitative (MAE of 1.18 ± 0.09 U) and qualitative metrics from a blinded review. Additionally, we conducted a single-arm, patient-blinded, proof-of-concept feasibility trial in 16 patients with T2D. The primary outcome was difference in mean daily capillary blood glucose during the trial, which decreased from 11.1 (±3.6) to 8.6 (±2.4) mmol L -1 (P < 0.01), meeting the pre-specified endpoint. No episodes of severe hypoglycemia or hyperglycemia with ketosis occurred. These preliminary results warrant further investigation in larger, more diverse clinical studies. ClinicalTrials.gov registration: NCT05409391 .
Keyphrases
- glycemic control
- blood glucose
- type diabetes
- artificial intelligence
- study protocol
- deep learning
- phase iii
- healthcare
- phase ii
- clinical trial
- weight loss
- machine learning
- insulin resistance
- case report
- big data
- primary care
- randomized controlled trial
- placebo controlled
- systematic review
- physical activity
- skeletal muscle
- early onset
- open label
- blood pressure
- double blind
- high resolution
- adipose tissue
- diabetic rats
- oxidative stress
- drug induced